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Job DescriptionAbout TravertineTravertine is a Climate Tech start-up based in Boulder, CO, that is rapidly scaling a technology for low-waste, carbon-negative production of critical elements, focusing on phosphoric acid production for our go-to-market application. Our electrochemical process converts phosphate rock into phosphoric acid for EV batteries and fertilizers, while simultaneously converting carbon dioxide captured from the air into a mineral addition to cement. Travertine was spun out of UC Berkeley in 2022 to scale this process to gigatons of permanent CDR while massively reducing industrial waste. Since its founding, Travertine has raised over $25M in capital, including over $5M in US Federal and State government grants. As one of the first companies to receive pre-purchases of CDR from the new Stripe-led $1B Frontier fund, and as founding members of the Carbon Removal Alliance, we are committed to industrial decarbonization at scale. We were named C&EN 10 startups to watch in 2022, a Bloomberg NEF Pioneer in 2023, and RMI Third Derivative 1st Gigaton Captured program participants in 2024. Today we are focused on scaling up commercial deployments of our technology, starting with a Demonstration Plant that is being installed in Ontario, NY. We believe in developing practical approaches to solving the climate crisis. The RoleTravertine is seeking a highly motivated and safety-conscious Operator to be part of the team operating our first-of-a-kind Demonstration Plant. This role involves close collaboration with other operators, engineers, and the R&D team to maintain steady operation while acquiring the critical data needed to verify carbon dioxide removal and inform the commercial design. Tasks will include equipment operation and maintenance, solution preparation, sample collection, sample analysis, waste neutralization and disposal, and other tasks as needed. Ability to troubleshoot process equipment and process issues is critical for this role. If you want to be part of a high-performing team starting up and operating a first-of-a-kind sustainable chemical process, this is the role for you. Key Responsibilities • Operate a wide range of chemical processing equipment, including but not limited to reactors, pumps, heat exchangers, and filtration systems., • Follow standard operating procedures (SOPs), batch records, and safety protocols to conduct chemical processes., • Monitor process variables and make adjustments to ensure safe and optimal operation., • Collect samples, perform chemical analyses, record accurate and detailed operational data and observations during runs., • Perform routine equipment maintenance, cleaning, and calibrations., • Collaborate with engineers, chemists, and other technical staff to execute test plans and experiments., • Assist in the setup and teardown of process equipment and systems for various campaigns., • Troubleshoot equipment and process issues and report findings to engineering staff., • Maintain a clean, organized, and safe working environment in compliance with company policies and regulatory standards., • Participate in safety audits, process hazard analyses, and continuous improvement initiatives.Qualifications, • Associate's degree in Process Technology, Chemical Technology, Industrial Technology, Chemistry, Materials Science, or related field, • 0-2 years’ experience as a technician building, maintaining, and operating chemical equipment, • Experience with wet chemistry laboratory work and sample analysis, • Strong mechanical aptitude and familiarity with chemical processing equipment., • Basic understanding of process control systems and instrumentation., • Ability to interpret technical documents such as P&IDs, batch sheets, and MSDSs., • Excellent attention to detail and strong organizational skills., • Ability to work independently and as part of a multidisciplinary team., • Flexibility to work shifts, nights, weekends, or extended hours as needed. Note the plant will operate 24/7.Benefits, • Competitive pay, • Health, Dental, Vision, Life Insurance, • 401k with 100% match up to 3% of salary, • Flexible time off policy We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Job Description Kelly® Science & Clinical is seeking a Chemist for our client in Rochester, New York. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts. Schedule: On-site Monday through Friday 8am to 5pm Length of assignment: ~1 year contract Pay: $21-27 an hour Depending on experience Recent grads welcome to apply! The applicant will be responsible for the testing of medical devices, stability samples and validation samples using existing analytical chromatography methods and wet chemistry techniques. This position is part of the R D team with responsibility for product characterization for biocompatibility and product improvement. Responsibilities: • Responsible for conducting and executing tests and experiments using both established methods and newly developed/novel techniques Independently operate analytical instruments such as an HPLC, GC, FTIR, UV-Vis, etc. to generate data., • Record and report all lab data as per approved procedures and regulatory requirements., • Analyze and critique results, noting significant deviations from the expected results., • Troubleshoot experiments and instrumentation., • Learn and understand new experimental techniques with a curiosity to apply them for unique project/assignment requirements., • Maintain a clean and safe work environment in the laboratory., • Ensure all work is performed and documented in accordance with existing company policies, procedures, current Good Manufacturing Practices, and health and safety requirements.Requirements:, • BA/BS in Chemistry or related field Knowledge of various chromatographic techniques including liquid chromatography and gas chromatography, • Strong lab skills with strong undergrad experience and 0-3 years of industry experience, • Strong writing skills Excellent team player with good organizational, interpersonal and communications skills, • Experience in chromatography a plus, • Experience with bio-medical research and development, and biocompatibility of medical devices a plusWhat happens next Once you apply, you’ll proceed to the next steps if your skills and experience look like a good fit. But don’t worry—even if this position doesn’t work out, you’re still in our network. That means all of our recruiters will have access to your profile, expanding your opportunities even more. Helping you discover what’s next in your career is what we’re all about, #P1 As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community. Why Kelly® Science & Clinical? Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed. About Kelly Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year. Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice.

We are looking for an experienced Health, Safety and Environmental Manager to oversee an HSE technical team supporting Kodak’s Specialty Chemicals, Inks and Dispersions manufacturing, as well as Solvent Recovery operations. The technical team provides direct, operational HSE support services, with particular focus on environmental compliance and reporting, as well as utilizing process safety risk management tools to identify and mitigate hazards associated with chemical manufacturing operations. This is an onsite role in Rochester, New York. As the Health, Safety and Environmental Manager you will focus on preventing pollution and providing a safe and healthy workplace for Kodak employees and others. You will report to the Senior Manager HSE Kodak Rochester, implementing strategies to ensure manufacturing operations comply with regulatory requirements, conform to internal standards, and meet sustainability objectives. You will lead a team of HSE Specialists and others who work to integrate the HSE compliance & internal standard requirements into Kodak chemical manufacturing and solvent recovery operations. These operations span multiple buildings and include 24/7 operations, over 200 employees and ten supervisors. The successful candidate must actively engage with cross-functional peers in HSE, HR, Operations, and Facilities, to address workplace health, safety and environmental concerns and improve overall performance. Compensation is commensurate with experience and qualifications. Responsibilities include (but are not limited to) the following: 1. Lead a team of technical HSE staff who provide direct support to manufacturing operations. Oversee staff meetings, regularly interact through 1:1 meetings, and conduct performance reviews., 2. Provide active support, coaching, feedback and professional development planning, with the goal of preparing team members to assume increased responsibilities., 3. Actively partner with the manufacturing operations leadership team; guide managers and group leaders across all functions to be effective HSE leaders/coaches in their respective positions., 4. Work closely with operations leadership to define HSE priorities and develop and track key performance indicators (KPIs) related to workplace health and safety, and environmental performance., 5. Communicate routinely with operations leadership on significant HSE issues, including implementation of new regulations, ISO requirements, progress on annual HSE goals and government agency inspection results., 6. In concert with Kodak HSE and operational leadership teams, actively manage implementation of workplace health and safety and environmental program improvements and support Process Safety Management reviews and change management activities., 7. Support the launch and integration of cloud-based incident reporting, action tracking and concern reporting software systems. Ensure root cause and corrective actions are identified to prevent the recurrence of HSE-related incidents., 8. Define HSE compliance training requirements and collaborate with Learning and Development staff to guide the structure and content of employee training programs. Requirements: • Strong knowledge of chemical manufacturing processes. Previous direct experience with Process Safety Management (PSM) regulated operations strongly preferred., • Working knowledge of occupational health and safety regulations and requirements at the local, state and federal levels., • Working knowledge of environmental regulations and requirements at the local, state and federal levels., • Knowledge and experience with ISO management systems (e.g. ISO 14001, ISO 45001); leadership of management review, auditing and corrective action processes preferred., • Demonstrated, effective team leadership skills with HSE technical staff., • Proven ability to work effectively in a cross-functional manner and build relationships., • Able to organize and coordinate multiple requirements/projects/processes simultaneously., • Able to complete responsibilities in a timely, professional, and quality manner., • Able to analyze complex problems, search out relevant information and gauge its importance when making decisions., • Effective written and oral communication skills; able to express oneself clearly and in technical and non-technical terms., • Excellent computer skills including advanced Excel (macros, pivot tables & formulas). Knowledge of Power BI and cloud-based HSE management software systems (e.g. VelocityEHS, Benchmark Gensuite) preferred. Education and Experience: • Minimum Bachelor’s degree, preferably in Occupational Safety and Health, Environmental or Chemical Engineering, Chemistry, or related field., • 5+ years of relevant experience leading HSE technical staff and overseeing HSE activities in a hazardous chemical environment, Process Safety Management regulated operations preferred., • Attained or actively pursuing professional occupational health and safety, environmental or engineering certification (e.g. CSP, CIH, CHMM, PE, etc.)

Kodak is seeking a Process Chemist/Engineer to join our Specialty Chemicals team in Rochester, NY to support large scale batch chemical manufacturing through a process engineering lens. The Process Chemist serves as the subject matter expert for assigned products and key technical resource for operations, leveraging engineering principles and data-driven methodologies to optimize process performance, improve efficiency, and enhance product quality. This role is responsible for troubleshooting and resolving process issues, identifying and implementing continuous improvement opportunities, commercializing new manufacturing processes, and ensuring safe, reliable, and cost-effective production of specialty chemicals for internal and external customers. The Process Chemist role offers an exciting opportunity to work at the intersection of synthetic chemistry and process engineering. Key Responsibilities: • Subject matter expert and process owner of assigned manufacturing portfolio., • Responsible for quality and yield of assigned processes. Processes include synthetic organic chemistry, synthetic inorganic chemistry, polymer chemistry, and formulation chemistry., • Apply Lean Six Sigma tools (DMAIC, statistical analysis, process capability, trend analysis, control charting, etc.) to reduce variability and improve yield, quality, throughput, and cycle time., • Lead or support continuous improvement initiatives targeting waste reduction, cost savings, productivity gains, quality improvement, and safety improvements., • Lead root cause investigations using structured problem-solving methods (e.g., 5Y, 5M, FMEA) for non-conforming materials and implement sustainable corrective and preventive actions., • Manage job specific projects assigned by job function or supervision., • Maintain document control of all assigned process write-ups., • Develop and author manufacturing processes, process design, control strategies, and operating procedures., • Follow and improve division procedures in accordance with ISO 9001 standards., • Act as production lead for the scale-up of chemical processes from laboratory and pilot to full manufacturing scale., • Ensure processes are designed and operated in compliance with safety, environmental, and regulatory requirements., • Participate in process hazard analyses (PHA), process safety review (PSR), management of change (MOC), and risk assessments., • Develop and maintain working knowledge of plant and process operating equipment., • Understand and estimate cost structures of assigned products and monitor production variance against standard., • Communicate effectively in writing and verbally within and across departments and to site management., • Serve as a technical resource for plant operations, providing real-time support for process deviations and upsets., • Must be willing to support 24/7 plant operations. Monday – Friday, 40+ hours with typical day staff schedule. Evening and weekend support as needed. Required Skills/Experience: • Bachelor’s in Chemistry with 2+ years of industrial experience or Master’s in Chemistry with 0+ years of industrial experience. Candidates with a Bachelor’s in Chemical Engineering with batch chemical manufacturing experience will also be considered., • Experience with process scale-up, plant operations, or commercialization preferred., • Strong understanding of synthetic and analytical chemistry., • Structured problem-solving and critical thinking., • Must be detail-oriented, self-motivated, and able to work independently., • Ability to complete multiple tasks quickly and efficiently., • Ability to work on the production floor., • Strong interpersonal skills., • Effective written and verbal communication skills., • Working knowledge in Microsoft Office Suite (Excel, Outlook, Word). Desired Skills/Experience: • Previous or current experience working in a large-scale chemical manufacturing environment is a benefit., • Experience applying Lean Six Sigma tools (Green Belt or higher preferred)., • Experience with ISO 9001 is preferred., • Experience with project management preferred., • Skilled in problem solving and diagnostic troubleshooting., • Proficiency in data analysis (e.g., Excel, JMP, etc.), • Mechanically inclined.

Eastman Kodak is looking for a Development Technician to join our Printed Electronics team onsite in Rochester NY, reporting to the VP of Printed Electronics. The printed electronics manufacturing process utilizes production-scale, roll-to-roll equipment in class 1,000 and 10,000 cleanroom environments. The equipment is used for the development and manufacturing of patterned conductive films using two fundamental process blocks: 1) flexographic printing and 2) electroless copper plating. The scope of this position includes supporting R&D activities in the field of flexographic printing, which could ultimately be adopted in a manufacturing-scale process. The right candidate will be able to independently manage day-to-day work loads – including executing lab-scale printing and mixing experiments for ink formulation. Responsibilities: • Hands-on R&D scale flexographic printing, • Work directly with the scientific staff to scope, draft and execute experiments, • Optical, physical and electrical evaluation of printed and plated samples, • Work with the Product Development Director to drive technology from R&D to manufacturing Preferred Skills: • Experience executing bench-scale experiments, such as ink handling, dispersions and/or emulsion formulation understanding, hands-on capability in mixing, chemical handling, printing; coating; print/coating evaluation, • Experience with optical microscopy and visual inspection techniques, • Experience in DC electrical measurements, such as resistance testing, • Data entry and experimental record keeping, • Proficient with Microsoft Excel, PowerPoint, and Word, • Experience working on cross-functional teams, • Good laboratory practices Educational and Experience Requirements: • A.S. Degree in Chemistry/related field OR equivalent experience in flexographic printing, ink formulation and chemistry laboratory best practices., • Would consider recent graduate with co-op/internship experience or candidate with industry experience.

Kodak is seeking a Process Chemist/Engineer to join our Specialty Chemicals team in Rochester, NY to support large scale batch chemical manufacturing through a process engineering lens. The Process Chemist serves as the subject matter expert for assigned products and key technical resource for operations, leveraging engineering principles and data-driven methodologies to optimize process performance, improve efficiency, and enhance product quality. This role is responsible for troubleshooting and resolving process issues, identifying and implementing continuous improvement opportunities, commercializing new manufacturing processes, and ensuring safe, reliable, and cost-effective production of specialty chemicals for internal and external customers. The Process Chemist role offers an exciting opportunity to work at the intersection of synthetic chemistry and process engineering. Key Responsibilities: • Subject matter expert and process owner of assigned manufacturing portfolio., • Responsible for quality and yield of assigned processes. Processes include synthetic organic chemistry, synthetic inorganic chemistry, polymer chemistry, and formulation chemistry., • Apply Lean Six Sigma tools (DMAIC, statistical analysis, process capability, trend analysis, control charting, etc.) to reduce variability and improve yield, quality, throughput, and cycle time., • Lead or support continuous improvement initiatives targeting waste reduction, cost savings, productivity gains, quality improvement, and safety improvements., • Lead root cause investigations using structured problem-solving methods (e.g., 5Y, 5M, FMEA) for non-conforming materials and implement sustainable corrective and preventive actions., • Manage job specific projects assigned by job function or supervision., • Maintain document control of all assigned process write-ups., • Develop and author manufacturing processes, process design, control strategies, and operating procedures., • Follow and improve division procedures in accordance with ISO 9001 standards., • Act as production lead for the scale-up of chemical processes from laboratory and pilot to full manufacturing scale., • Ensure processes are designed and operated in compliance with safety, environmental, and regulatory requirements., • Participate in process hazard analyses (PHA), process safety review (PSR), management of change (MOC), and risk assessments., • Develop and maintain working knowledge of plant and process operating equipment., • Understand and estimate cost structures of assigned products and monitor production variance against standard., • Communicate effectively in writing and verbally within and across departments and to site management., • Serve as a technical resource for plant operations, providing real-time support for process deviations and upsets., • Must be willing to support 24/7 plant operations. Monday – Friday, 40+ hours with typical day staff schedule. Evening and weekend support as needed. Required Skills/Experience: • Bachelor’s in Chemistry with 2+ years of industrial experience or Master’s in Chemistry with 0+ years of industrial experience. Candidates with a Bachelor’s in Chemical Engineering with batch chemical manufacturing experience will also be considered., • Experience with process scale-up, plant operations, or commercialization preferred., • Strong understanding of synthetic and analytical chemistry., • Structured problem-solving and critical thinking., • Must be detail-oriented, self-motivated, and able to work independently., • Ability to complete multiple tasks quickly and efficiently., • Ability to work on the production floor., • Strong interpersonal skills., • Effective written and verbal communication skills., • Working knowledge in Microsoft Office Suite (Excel, Outlook, Word). Desired Skills/Experience: • Previous or current experience working in a large-scale chemical manufacturing environment is a benefit., • Experience applying Lean Six Sigma tools (Green Belt or higher preferred)., • Experience with ISO 9001 is preferred., • Experience with project management preferred., • Skilled in problem solving and diagnostic troubleshooting., • Proficiency in data analysis (e.g., Excel, JMP, etc.), • Mechanically inclined.

Job Description Are you a self-driven person looking to advance your career as a high-impact player on a team? If so, we have an exciting challenge for you and your future! Our culture is built on value commitments to innovation, quality, results, integrity, community, people, and collaboration that fosters a strong employee engagement, teamwork, safety and wellness. We offer a competitive benefits package that includes health, dental, vision, wellness programs, employee discounts, retirement plans, tuition reimbursement, ongoing development, advancement opportunities and more. Founded in 1846, today HP Hood is one of the largest and most trusted food and beverage manufacturers in the United States. Our portfolio of national and super-regional brands and licensed products includes Hood, Heluva Good, Lactaid, Blue Diamond Almond Breeze, Planet Oat and more. The candidate hired for this position will support Sanitation Programs at our Fluid, Cultured, and Ice Cream plants, requiring approximately 70% travel to these facilities across New York State and New England. We are unable to offer relocation assistance or sponsorship at this time. Job Summary: The technical sanitation specialist will be responsible for providing technical support to all of HP Hood's facilities. This includes but is not limited to troubleshooting quality issues, optimizing CIP systems, standardizing CIPs and manual cleaning practices and providing additional training and support as deemed necessary. This position will work closely with the Sr. Manager, Strategic Sanitation Programs to establish long term strategic business plans, monitor corporate sanitation policies and help foster an environment of proactive sanitation across multiple departments and divisions. Essential Duties and Responsibilities: • Provide technical leadership and guidance to Operations Quality, R&D, and manufacturing facilities in the areas of sanitation, pathogen/environmental control, integrated pest control, new equipment design, installation or construction and other food safety or quality initiatives related to sanitation processes., • Assist in the development and implementation of strategic sanitation programs, policies, plans and processes to ensure that sanitary performance meets Hood standards as well as supports Food Safety requirements towards regulatory compliance. Assist in quality issue troubleshooting and root cause analysis., • Incorporate principles of dry as well as wet cleaning best practices, allergen management, and "allergen clean" vs. microbial clean as needed., • Utilize corporate Sanitation Standard Operating Procedures (SSOP's) as guidance, prepare plant specific SSOP's for equipment and processes. Ensure all SSOP forms and records are current and completed. Incorporate visual learning and step-by-step processes which are easily followed and comprehended by staff., • Communicate significant issues or developments identified during plant visits and provide recommended process improvements to management., • Prepare and present technical and program information to team members and management., • Directs technical and administrative workers engaged in sanitation activities., • Maintain a working knowledge of government and industry codes and standards., • Provide education and technical support to assure effective deployment and implementation of corporate sanitation and food safety policies and procedures., • Work cross functionally and collaboratively with all Plant Operations, Corporate QA, Food Safety, and Chemical Supply Vendors to implement and continuously improve on sanitation programs and policies., • Develop a culture of proactive quality. Education and Experience: • 5+ years of Quality Assurance experience in both corporate and plant locations., • Four-year degree preferred. Preferably a BS or BA in Food Science, Dairy Science, Biology or Chemistry Skills and Competencies: • Strong technical dairy knowledge, • Strong verbal & written skills, • Strong presentation delivery skills (written & delivery), • Strong interpersonal skills with a customer orientation (internal & external), • Strong computer skills (MS Office, BPCS, Formula System), • Experience with regulatory, third party, and customer audits, • Experience in successfully addressing environmental sanitation challenges in all areas of plant, • Thorough knowledge and experience with diverse sanitizing applications, • Certification and/or License – Preventive Controls Qualified Individual (PCQI) certification or attainment of PCQI within 6 months of hiring, • A general knowledge of food and environmental microbiological testing as well as preventative measures including sanitary design and automated sanitation and efficiency is required. The reasonably anticipated pay range for this position is $75,000 - $93,000. Exact compensation may vary based on skills, experience and location. #LI-GD1 #LI-Remote Exact compensation may vary based on skills, experience and location. The pay range for this position is$75,000—$93,000 USD HP Hood is an Equal Opportunity Employer Female/Minority/Veteran/Disabled "VERVRAA Federal Contractor" Privacy Policy CCPA For Applicants in Massachusetts - It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Employment is subject to verification of an applicant's identity and eligibility for employment in the United States as required by immigration laws. We are unable to assist with sponsorship at this time.

Kodak is looking for a Development Technician to join our Printed Electronics team in Rochester NY, reporting to the VP of Printed Electronics. The printed electronics manufacturing process utilizes production-scale, roll-to-roll equipment in class 1,000 and 10,000 cleanroom environments. The equipment is used for the development and manufacturing of patterned conductive films using two fundamental process blocks: 1) flexographic printing and 2) electroless copper plating. The scope of this position includes supporting R&D activities in the field of flexographic printing, which could ultimately be adopted in a manufacturing-scale process. The right candidate will be able to independently manage day-to-day work loads – including executing lab-scale printing and mixing experiments for ink formulation. Responsibilities: • Hands-on R&D scale flexographic printing, • Work directly with the scientific staff to scope, draft and execute experiments, • Optical, physical and electrical evaluation of printed and plated samples, • Work with the Product Development Director to drive technology from R&D to manufacturing Required Skills: • Experience executing bench-scale experiments, such as ink handling, dispersions and/or emulsion formulation understanding, hands-on capability in mixing, chemical handling, printing; coating; print/coating evaluation, • Experience with optical microscopy and visual inspection techniques, • Experience in DC electrical measurements, such as resistance testing, • Data entry and experimental record keeping, • Proficient with Microsoft Excel, PowerPoint, and Word, • Experience working on cross-functional teams, • Good laboratory practices Educational and Experience Requirements: • A.S. Degree in Chemistry or equivalent experience in flexographic printing, ink formulation and chemistry laboratory best practices.

Kodak is looking for a Senior Chemical Operator to work in our Specialty Chemical Division (SCID) Small Scale manufacturing department. This operator will synthesize various chemicals using traditional chemistry glassware (1L to 72L) and other chemical processing equipment while maximizing output, maintaining product quality, minimizing waste, and following all safety guidelines and manufacturing procedures. Specialized Skills and Job Expectations: • Synthesize chemicals using Small Scale manufacturing equipment at 1L to 72L size., • Strict adherence to division operation and HSE procedures., • Follow process procedures to run reactions from starting materials through synthesis of final products., • Plan workday to manage processes that may take hours or multiple days. Responsible for numerous types of unit operations., • Work with area Process/Development Chemists to resolve any quality or yield issues., • Participate in process quality/life guards as needed., • Participate in process safety reviews and process hazard analyses as needed., • Individual should have good interpersonal skills and the ability to work in a small team-oriented environment., • Good communication skills are needed, both written and verbal, with the ability to express oneself clearly, read job related material, and write effectively., • Basic computer skills including Microsoft Office and Lotus Notes., • Individual must be able to perform basic math functions., • Position requires working in walk-in fume hoods, standing, frequent lifting, carrying, pulling, pushing, etc., • Individual should have good analytical and trouble shooting skills., • Monday – Friday, 8 hour work schedule., • Willing to work overtime or adjust work schedule for shutdowns and business needs. Desired Skills/Experience: • 10+ years of chemical manufacturing experience, mechanically inclined, and chemical/technical experience., • Associates degree in chemistry/chemical technology or related field with 5+ years of experience will be considered., • Good interpretation of procedures and adherence to HSE and process procedures., • Understanding of continuous improvement and Lean Six Sigma techniques.

QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers with fast, accurate and consistent testing where and when they are needed most home to hospital, lab to clinic. Our culture puts our team members first and prioritizes actions that support happiness, inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all. As we continue to grow as QuidelOrtho, we are seeking an Operator II, Slides Manufacturing in the Slide Assembly Department. This position is responsible for quality and maintaining the highest standards in compliance within company policies, procedures and all applicable regulations. Accountable for adhering to all EHS guidelines. This position is located in Rochester, NY. Work Schedule: "Firemen's Rotation": Two 12 hour days (6:00am-6:00pm) followed by two 12 hour nights (6:00pm-6:00am) • Consistently meet production metrics on at least one piece of automated production machine with minimal supervision., • Assist in troubleshooting and repairing equipment., • Perform basic data entry, i.e. SAP, SPIDER, etc., • Perform basic quality checks and escalate as needed., • Participate in simple root cause analysis under supervision., • Follow and contribute to updates in SOPs, work instructions, and job plans., • Ability to perform basic machine adjustments under guidance of a senior operator., • Encourages positive relationships by utilizing effective communication skills., • Performs multiple job functions within the Work Center and willingly flexes as business needs dictate., • Identifies EH&S opportunities and provides recommendations., • Participates in implementation of solutions., • Aligns development with business needs., • Participates in cross training. Required Skills: • High school diploma or equivalent., • 1-3 years of hands-on experience in high-speed automated production, packaging, formulation process, and/or related systems., • Ability to work effectively in a team., • Application of basic safety practices in daily tasks., • Basic understanding of GMP requirements and adherence to them during manufacturing activities., • Completes training across multiple pieces of automated equipment., • Participation in basic root cause analysis exercises using methodologies such as 5 Whys and Fishbone Diagram. Additional Skills: • Intermediate math and communication skills., • Familiarity with basic tools and practices., • Basic problem-solving skills., • Basic knowledge of 5S and ability to apply concepts., • Ability to navigate through HMI screens., • Ability to recognize patterns of failures within an automated manufacturing line., • Understanding of basic GMP and compliance in a regulated industry., • Ability to complete paperwork with high accuracy following good documentation practices. Internal Partners: Maintenance, Engineering, Quality External Partners: Suppliers The work environment characteristics are representative of a manufacturing, laboratory, or warehouse environment and include handling of viral and bacterial hazards, potentially hazardous chemicals, as well as infectious or potentially infectious bodily fluids, tissues, and samples. Up to 75% of the time you will be, standing, walking or sitting for extended periods of time. Ability to lift up to 50 lbs. Flexible work hours to meet project deadlines. The salary range for this position takes into account a wide range of factors including education, experience, knowledge, skills, geography, and abilities of the candidate, in addition to internal equity and alignment with market data. At QuidelOrtho, it is not typical for an individual to be hired at or near the top range for their role and compensation decisions are dependent on the facts and circumstances of each case. The hourly range for this position is $20.00 to $27.00 hourly. QuidelOrtho offers a comprehensive benefits package including medical, dental, vision, life, and disability insurance, along with a 401(k) plan, employee assistance program, Employee Stock Purchase Plan, paid time off (including sick time), and paid Holidays. All benefits are non-contractual, and QuidelOrtho may amend, terminate, or enhance the benefits provided, as it deems appropriate. QuidelOrtho believes in Equal Opportunity for all and is committed to ensuring all individuals, including individuals with disabilities, have an opportunity to apply for those positions that they are interested in and qualify for without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, or any other protected characteristic. QuidelOrtho is also committed to providing reasonable accommodations to qualified individuals so that an individual can perform the duties. If you are interested in applying for an employment opportunity and require special assistance or an accommodation to apply due to a disability, please contact us at recruiting@quidelortho.com.

QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers with fast, accurate and consistent testing where and when they are needed most home to hospital, lab to clinic. Our culture puts our team members first and prioritizes actions that support happiness, inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all. As the company continues to grow, as one QuidelOrtho we are seeking a Manufacturing Engineer II to work in our Assay manufacturing facility. The Manufacturing Engineer II is an integral member of the Assay Manufacturing Engineering team. This position will support a 24x7 high speed automated manufacturing operation and the associated engineering and maintenance functions when required to troubleshoot high level issues when impacting production. Additionally, the Manufacturing Engineer shall perform engineering studies and analyses on existing manufacturing processes to improve process reliability, product quality, and cost. This position is expected to be capable of carrying out an important segment of a medium scoped engineering program with some complexity or a smaller program of limited complexity and scope. This position is in Rochester, NY. Schedule: Primary A shift, Monday - Friday; however, may require extended hours or weekend work to support the 24/7 operations or project deliverables. Conceives, plans, and implements solutions to technical problems requiring unconventional approaches, new designs, and equipment and process development. Keeps abreast of new technical developments affecting the organization for an assigned area of responsibility. Formulates strategies for the development of programs that bring new and improved engineering technology into the company; initiates, leads, and supports cost improvement projects and business continuity initiatives. Maintains clear communication with internal and external business partners regarding expectations, satisfaction, and/or quality of results. Initiate and facilitate continuous improvement activities including smaller scoped projects related to OEE and equipment obsolescence. Identifies new opportunities to increase equipment uptime and reduce business risk. Consults with maintenance to draft maintenance procedures for new designs, developing troubleshooting techniques, creation of preventative maintenance (PM) schedules, and providing recommended spare parts lists. Supports the implementation of new equipment and/or the modifications to existing to improve plant efficiency and performance yields. Required: BS in Engineering (BSME, BSEE or BET is preferred) with 5 years minimum work experience or MS with up to 3 years' demonstrated experience in Engineering. Strong electrical & mechanical aptitude with troubleshooting experience. Adept with Microsoft Office tools (e.g. Word, Excel, Project, PowerPoint, etc.). Ability to manage competing priorities in a results-driven environment is essential. Familiar with CAD tools (e.g. AutoCAD). Working knowledge and understanding of pneumatic systems and pneumatic logic. Executes the validation process, including conducting design reviews, pre-validation assessments, and installation, operational, and process qualifications. Preferred: Experience with motor drive systems, process controls systems, manufacturing equipment and vision systems. Control Networking experience (Ethernet/IP, DeviceNet, ControlNet), and familiarity with databases. Experience working in an FDA Medical Device Manufacturing Facility with associated FDA and ISO regulations. Internal Partners: Operations, Maintenance, Facilities and Environmental Health & Safety, Quality and Regulatory External Partners: Suppliers The work environment characteristics are representative of a manufacturing, laboratory, or warehouse environment and include handling of viral and bacterial hazards, potentially hazardous chemicals, as well as infectious or potentially infectious bodily fluids, tissues, and samples. Up to 75% of the time you will be, standing, walking or sitting for extended periods of time. Ability to lift up to 50 lbs. Flexible work hours to meet project deadlines. The salary range for this position takes into account a wide range of factors including education, experience, knowledge, skills, geography, and abilities of the candidate, in addition to internal equity and alignment with market data. At QuidelOrtho, it is not typical for an individual to be hired at or near the top range for their role and compensation decisions are dependent on the facts and circumstances of each case. The salary range for this position is $68,000 to $116,000 and is bonus eligible. QuidelOrtho offers a comprehensive benefits package including medical, dental, vision, life, and disability insurance, along with a 401(k) plan, employee assistance program, Employee Stock Purchase Plan, paid time off (including sick time), and paid Holidays. All benefits are non-contractual, and QuidelOrtho may amend, terminate, or enhance the benefits provided, as it deems appropriate. QuidelOrtho believes in Equal Opportunity for all and is committed to ensuring all individuals, including individuals with disabilities, have an opportunity to apply for those positions that they are interested in and qualify for without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, or any other protected characteristic. QuidelOrtho is also committed to providing reasonable accommodations to qualified individuals so that an individual can perform their duties. If you are interested in applying for an employment opportunity and require special assistance or an accommodation to apply due to a disability, please contact us at recruiting@quidelortho.com.

QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers with fast, accurate and consistent testing where and when they are needed most home to hospital, lab to clinic. Our culture puts our team members first and prioritizes actions that support happiness, inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all. As we continue to grow as QuidelOrtho, we are seeking a Quality Engineer II. The Quality Engineer II will provide quality engineering support to Quality and Operations staff on all aspects of the manufacturing process at the Rochester Manufacturing Site. The candidate will work to resolve nonconformances by ensuring adequate RCIs are conducted and effective CAPAs are implemented. The candidate will utilize key Quality Engineering principles, tools, and practices to develop and optimize process controls and quality system processes and identify opportunities to improve quality and cost that are aligned with the overall business goals and Ortho's Quality Policy. The candidate will accurately assess risk and will drive quality related decisions. This opportunity is located in Rochester, NY. Partner with operations to evaluate and address quality events including nonconformances, product dispositions, root cause investigations, and implement appropriate CAPA based on risk level. Analyze and monitor key quality metrics and develop action plans to address unfavorable trends. Promote continuous improvement activities by seeking out opportunities to optimize processes and systems to reduce variation and improve product quality. Drive implementation of best practices to eliminate repeat quality events and improve product quality. Support product and process root cause investigations by collaborating with product support, engineering, and operations. Support and participate in inspection readiness activities by applying working knowledge of ISO13485 and 21CFR Part 820 regulations. Provide coaching, training, and technical guidance to business partners in aspects of the company quality system requirements as they pertain to manufacturing quality and provide guidance of effectively applying key quality engineering principles and tools. Perform other work-related duties as assigned Required: B.S. Degree in Chemistry, Biochemistry, Biology, Engineering, or a related discipline. 3-5 years of experience in Quality in a highly regulated manufacturing environment (Diagnostics, Medical Device, Pharmaceutical, or Consumer). Advanced Microsoft Office (Word, Excel, PowerPoint, etc.) tools experience for communications, reporting and data analysis. Preferred: Clearly and effectively documents, communicates, and presents technical information. Works effectively independently as well with a cross-functional team across Operations, Product Support, Compliance, Regulatory, and Suppliers. Demonstrates a high degree of accuracy and attention to details Strong organization and time management skills. Analytical and problem-solving skills with an ability to use scientific knowledge and statistical methods to identify and resolve issues. Knowledge of current and applicable GMP regulations including ISO13485 and 21 CFR Part 820 Internal Partners: Operations, Engineering, Product Support, Laboratory Personnel, Regulatory Affairs, and Compliance External Partners: Regulatory Agencies The work environment characteristics are representative of a manufacturing, laboratory, or warehouse environment and include handling of viral and bacterial hazards, potentially hazardous chemicals, as well as infectious or potentially infectious bodily fluids, tissues, and samples. Working around moving machinery. Protective equipment required, as needed. The salary range for this position takes into account a wide range of factors including education, experience, knowledge, skills, geography, and abilities of the candidate, in addition to internal equity and alignment with market data. At QuidelOrtho, it is not typical for an individual to be hired at or near the top range for their role and compensation decisions are dependent on the facts and circumstances of each case. The salary range is $8,000.00 to $116,000.00 and is bonus eligible. QuidelOrtho offers a comprehensive benefits package including medical, dental, vision, life, and disability insurance, along with a 401(k) plan, employee assistance program, Employee Stock Purchase Plan, paid time off (including sick time), and paid Holidays. All benefits are non-contractual, and QuidelOrtho may amend, terminate, or enhance the benefits provided, as it deems appropriate. QuidelOrtho believes in Equal Opportunity for all and is committed to ensuring all individuals, including individuals with disabilities, have an opportunity to apply for those positions that they are interested in and qualify for without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, or any other protected characteristic. QuidelOrtho is also committed to providing reasonable accommodations to qualified individuals so that an individual can perform their duties. If you are interested in applying for an employment opportunity and require special assistance or an accommodation to apply due to a disability, please contact us at orthorecruiting@orthoclinicaldiagnostics.com or ecruiting@quidelortho.com. #LI-SP1

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